Neuroprotective effects of riluzole in early phase Parkinson's disease on clinically relevant parameters in the marmoset MPTP model
The present study evaluates neuroprotection in a marmoset MPTP (1-methyl-1,2,3,6-tetrahydropyridine) model representing early Parkinson's disease (PD). The anti-glutamatergic compound riluzole is used as a model compound for neuroprotection. The compound is one of the few protective compounds u...
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description | The present study evaluates neuroprotection in a marmoset MPTP (1-methyl-1,2,3,6-tetrahydropyridine) model representing early Parkinson's disease (PD). The anti-glutamatergic compound riluzole is used as a model compound for neuroprotection. The compound is one of the few protective compounds used in the clinic for a neurodegenerative disorder.
Marmoset monkeys were randomized into three groups of six: 1) an MPTP group receiving a total MPTP dose of 7 mg/kg (4 injections over two weeks, s.c.) 2) a riluzole group receiving besides MPTP, a twice daily dose of riluzole (10 mg/kg, p.o.), starting one week before MPTP and continuing for one week after the final MPTP injection and 3) a control group receiving saline instead of MPTP and riluzole. The marmosets' Parkinsonian symptoms were scored daily and their activity level, hand-eye coordination, jumping behavior, axial turning and night sleep parameters were tested and recorded weekly. At three weeks following the last MPTP challenge, brains were dissected and dopamine levels in the striatum and the tyrosine hydroxylase (TH) expressing dopamine (DA) neurons in the substantia nigra (SN) were compared. MPTP affected all behavioral parameters and sleep architecture and induced a relatively mild (50%) decline of DA neurons in the substantia nigra (SN). Riluzole relieved the Parkinsonian signs, and improved the hand-eye coordination as well as turning ability. Moreover, riluzole prevented the impact of MPTP on sleep architecture and rapid eye movement behavioral disorder (RBD). Riluzole also increased the number of surviving DA neurons in MPTP-treated marmosets to 75%. However, riluzole did not prevent the MPTP-induced impairments on locomotor activity and jumping activity.
In conclusion, reduction of excitotoxicity by riluzole appeared to be effective in reducing progressive neurodegeneration and relieved several clinically relevant PD symptoms in an animal model representing the early phase of PD.
► Marmoset MPTP model for early Parkinson's disease. ► Riluzole protects against behavior and sleep symptoms. ► Riluzole protects against low level neurodegeneration. ► Overview of neuroprotective effects on behavior, sleep and neuron survival. |
doi_str_mv | 10.1016/j.neuropharm.2011.11.016 |
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Marmoset monkeys were randomized into three groups of six: 1) an MPTP group receiving a total MPTP dose of 7 mg/kg (4 injections over two weeks, s.c.) 2) a riluzole group receiving besides MPTP, a twice daily dose of riluzole (10 mg/kg, p.o.), starting one week before MPTP and continuing for one week after the final MPTP injection and 3) a control group receiving saline instead of MPTP and riluzole. The marmosets' Parkinsonian symptoms were scored daily and their activity level, hand-eye coordination, jumping behavior, axial turning and night sleep parameters were tested and recorded weekly. At three weeks following the last MPTP challenge, brains were dissected and dopamine levels in the striatum and the tyrosine hydroxylase (TH) expressing dopamine (DA) neurons in the substantia nigra (SN) were compared. MPTP affected all behavioral parameters and sleep architecture and induced a relatively mild (50%) decline of DA neurons in the substantia nigra (SN). Riluzole relieved the Parkinsonian signs, and improved the hand-eye coordination as well as turning ability. Moreover, riluzole prevented the impact of MPTP on sleep architecture and rapid eye movement behavioral disorder (RBD). Riluzole also increased the number of surviving DA neurons in MPTP-treated marmosets to 75%. However, riluzole did not prevent the MPTP-induced impairments on locomotor activity and jumping activity.
In conclusion, reduction of excitotoxicity by riluzole appeared to be effective in reducing progressive neurodegeneration and relieved several clinically relevant PD symptoms in an animal model representing the early phase of PD.
► Marmoset MPTP model for early Parkinson's disease. ► Riluzole protects against behavior and sleep symptoms. ► Riluzole protects against low level neurodegeneration. ► Overview of neuroprotective effects on behavior, sleep and neuron survival.</description><identifier>ISSN: 0028-3908</identifier><identifier>EISSN: 1873-7064</identifier><identifier>DOI: 10.1016/j.neuropharm.2011.11.016</identifier><identifier>PMID: 22178201</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Animals ; Behavior ; Callithrix ; Corpus Striatum - drug effects ; Corpus Striatum - metabolism ; Dopamine ; Dopamine - metabolism ; Dopaminergic Neurons - drug effects ; Dopaminergic Neurons - metabolism ; Female ; Male ; Marmoset ; MPTP ; MPTP Poisoning - drug therapy ; Neuroprotective Agents - pharmacology ; Neuroprotective Agents - therapeutic use ; Parkinson's disease ; Riluzole ; Riluzole - pharmacology ; Riluzole - therapeutic use ; Sleep ; Substantia Nigra - drug effects ; Substantia Nigra - metabolism</subject><ispartof>Neuropharmacology, 2012-03, Vol.62 (4), p.1700-1707</ispartof><rights>2011 Elsevier Ltd</rights><rights>Copyright © 2011 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c471t-1809fdc676d2f26a5da74e17470d8124c63b0f3e629aabaed99469c254ffa23e3</citedby><cites>FETCH-LOGICAL-c471t-1809fdc676d2f26a5da74e17470d8124c63b0f3e629aabaed99469c254ffa23e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0028390811004953$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22178201$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Verhave, Peternella S.</creatorcontrib><creatorcontrib>Jongsma, Marjan J.</creatorcontrib><creatorcontrib>Van Den Berg, Roland M.</creatorcontrib><creatorcontrib>Vanwersch, Raymond A.P.</creatorcontrib><creatorcontrib>Smit, August B.</creatorcontrib><creatorcontrib>Philippens, Ingrid H.C.H.M.</creatorcontrib><title>Neuroprotective effects of riluzole in early phase Parkinson's disease on clinically relevant parameters in the marmoset MPTP model</title><title>Neuropharmacology</title><addtitle>Neuropharmacology</addtitle><description>The present study evaluates neuroprotection in a marmoset MPTP (1-methyl-1,2,3,6-tetrahydropyridine) model representing early Parkinson's disease (PD). The anti-glutamatergic compound riluzole is used as a model compound for neuroprotection. The compound is one of the few protective compounds used in the clinic for a neurodegenerative disorder.
Marmoset monkeys were randomized into three groups of six: 1) an MPTP group receiving a total MPTP dose of 7 mg/kg (4 injections over two weeks, s.c.) 2) a riluzole group receiving besides MPTP, a twice daily dose of riluzole (10 mg/kg, p.o.), starting one week before MPTP and continuing for one week after the final MPTP injection and 3) a control group receiving saline instead of MPTP and riluzole. The marmosets' Parkinsonian symptoms were scored daily and their activity level, hand-eye coordination, jumping behavior, axial turning and night sleep parameters were tested and recorded weekly. At three weeks following the last MPTP challenge, brains were dissected and dopamine levels in the striatum and the tyrosine hydroxylase (TH) expressing dopamine (DA) neurons in the substantia nigra (SN) were compared. MPTP affected all behavioral parameters and sleep architecture and induced a relatively mild (50%) decline of DA neurons in the substantia nigra (SN). Riluzole relieved the Parkinsonian signs, and improved the hand-eye coordination as well as turning ability. Moreover, riluzole prevented the impact of MPTP on sleep architecture and rapid eye movement behavioral disorder (RBD). Riluzole also increased the number of surviving DA neurons in MPTP-treated marmosets to 75%. However, riluzole did not prevent the MPTP-induced impairments on locomotor activity and jumping activity.
In conclusion, reduction of excitotoxicity by riluzole appeared to be effective in reducing progressive neurodegeneration and relieved several clinically relevant PD symptoms in an animal model representing the early phase of PD.
► Marmoset MPTP model for early Parkinson's disease. ► Riluzole protects against behavior and sleep symptoms. ► Riluzole protects against low level neurodegeneration. ► Overview of neuroprotective effects on behavior, sleep and neuron survival.</description><subject>Animals</subject><subject>Behavior</subject><subject>Callithrix</subject><subject>Corpus Striatum - drug effects</subject><subject>Corpus Striatum - metabolism</subject><subject>Dopamine</subject><subject>Dopamine - metabolism</subject><subject>Dopaminergic Neurons - drug effects</subject><subject>Dopaminergic Neurons - metabolism</subject><subject>Female</subject><subject>Male</subject><subject>Marmoset</subject><subject>MPTP</subject><subject>MPTP Poisoning - drug therapy</subject><subject>Neuroprotective Agents - pharmacology</subject><subject>Neuroprotective Agents - therapeutic use</subject><subject>Parkinson's disease</subject><subject>Riluzole</subject><subject>Riluzole - pharmacology</subject><subject>Riluzole - therapeutic use</subject><subject>Sleep</subject><subject>Substantia Nigra - drug effects</subject><subject>Substantia Nigra - metabolism</subject><issn>0028-3908</issn><issn>1873-7064</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUUtvVCEUJkZjx-pfMOy6uiOvcmGpjVWTqrOoa8LAIWXkwgj3TlK3_nEZp-qyyUkg53wPDh9CmJI1JVS-2a0zLLXs72yd1oxQuu7VB0_QiqqRDyOR4ilaEcLUwDVRZ-hFaztCiFBUPUdnjNFRdd4K_fryR6iWGdwcD4AhhH5ruARcY1p-lgQ4Zgy2pnvcDRvgja3fY24lXzTsY4Njr2TsUszR2dRxFRIcbJ7x3lY7wQy1HUXmO8BTf3JpMOPPm9sNnoqH9BI9CzY1ePVwnqNv1-9vrz4ON18_fLp6ezM4MdJ5oIro4J0cpWeBSXvp7SiAjmIkXlEmnORbEjhIpq3dWvBaC6kduxQhWMaBn6OLk25f98cCbTZTbA5SshnK0oxmnGrJuXwcSTVjQjLVkeqEdLW0ViGYfY19x3tDiTlmZXbmf1bmmJXp1Qed-vrBZNlO4P8R_4bTAe9OAOifcohQTXMRsgMfa8_I-BIfd_kN9patXg</recordid><startdate>201203</startdate><enddate>201203</enddate><creator>Verhave, Peternella S.</creator><creator>Jongsma, Marjan J.</creator><creator>Van Den Berg, Roland M.</creator><creator>Vanwersch, Raymond A.P.</creator><creator>Smit, August B.</creator><creator>Philippens, Ingrid H.C.H.M.</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7TK</scope></search><sort><creationdate>201203</creationdate><title>Neuroprotective effects of riluzole in early phase Parkinson's disease on clinically relevant parameters in the marmoset MPTP model</title><author>Verhave, Peternella S. ; Jongsma, Marjan J. ; Van Den Berg, Roland M. ; Vanwersch, Raymond A.P. ; Smit, August B. ; Philippens, Ingrid H.C.H.M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c471t-1809fdc676d2f26a5da74e17470d8124c63b0f3e629aabaed99469c254ffa23e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Animals</topic><topic>Behavior</topic><topic>Callithrix</topic><topic>Corpus Striatum - drug effects</topic><topic>Corpus Striatum - metabolism</topic><topic>Dopamine</topic><topic>Dopamine - metabolism</topic><topic>Dopaminergic Neurons - drug effects</topic><topic>Dopaminergic Neurons - metabolism</topic><topic>Female</topic><topic>Male</topic><topic>Marmoset</topic><topic>MPTP</topic><topic>MPTP Poisoning - drug therapy</topic><topic>Neuroprotective Agents - pharmacology</topic><topic>Neuroprotective Agents - therapeutic use</topic><topic>Parkinson's disease</topic><topic>Riluzole</topic><topic>Riluzole - pharmacology</topic><topic>Riluzole - therapeutic use</topic><topic>Sleep</topic><topic>Substantia Nigra - drug effects</topic><topic>Substantia Nigra - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Verhave, Peternella S.</creatorcontrib><creatorcontrib>Jongsma, Marjan J.</creatorcontrib><creatorcontrib>Van Den Berg, Roland M.</creatorcontrib><creatorcontrib>Vanwersch, Raymond A.P.</creatorcontrib><creatorcontrib>Smit, August B.</creatorcontrib><creatorcontrib>Philippens, Ingrid H.C.H.M.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Neurosciences Abstracts</collection><jtitle>Neuropharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Verhave, Peternella S.</au><au>Jongsma, Marjan J.</au><au>Van Den Berg, Roland M.</au><au>Vanwersch, Raymond A.P.</au><au>Smit, August B.</au><au>Philippens, Ingrid H.C.H.M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neuroprotective effects of riluzole in early phase Parkinson's disease on clinically relevant parameters in the marmoset MPTP model</atitle><jtitle>Neuropharmacology</jtitle><addtitle>Neuropharmacology</addtitle><date>2012-03</date><risdate>2012</risdate><volume>62</volume><issue>4</issue><spage>1700</spage><epage>1707</epage><pages>1700-1707</pages><issn>0028-3908</issn><eissn>1873-7064</eissn><abstract>The present study evaluates neuroprotection in a marmoset MPTP (1-methyl-1,2,3,6-tetrahydropyridine) model representing early Parkinson's disease (PD). The anti-glutamatergic compound riluzole is used as a model compound for neuroprotection. The compound is one of the few protective compounds used in the clinic for a neurodegenerative disorder.
Marmoset monkeys were randomized into three groups of six: 1) an MPTP group receiving a total MPTP dose of 7 mg/kg (4 injections over two weeks, s.c.) 2) a riluzole group receiving besides MPTP, a twice daily dose of riluzole (10 mg/kg, p.o.), starting one week before MPTP and continuing for one week after the final MPTP injection and 3) a control group receiving saline instead of MPTP and riluzole. The marmosets' Parkinsonian symptoms were scored daily and their activity level, hand-eye coordination, jumping behavior, axial turning and night sleep parameters were tested and recorded weekly. At three weeks following the last MPTP challenge, brains were dissected and dopamine levels in the striatum and the tyrosine hydroxylase (TH) expressing dopamine (DA) neurons in the substantia nigra (SN) were compared. MPTP affected all behavioral parameters and sleep architecture and induced a relatively mild (50%) decline of DA neurons in the substantia nigra (SN). Riluzole relieved the Parkinsonian signs, and improved the hand-eye coordination as well as turning ability. Moreover, riluzole prevented the impact of MPTP on sleep architecture and rapid eye movement behavioral disorder (RBD). Riluzole also increased the number of surviving DA neurons in MPTP-treated marmosets to 75%. However, riluzole did not prevent the MPTP-induced impairments on locomotor activity and jumping activity.
In conclusion, reduction of excitotoxicity by riluzole appeared to be effective in reducing progressive neurodegeneration and relieved several clinically relevant PD symptoms in an animal model representing the early phase of PD.
► Marmoset MPTP model for early Parkinson's disease. ► Riluzole protects against behavior and sleep symptoms. ► Riluzole protects against low level neurodegeneration. ► Overview of neuroprotective effects on behavior, sleep and neuron survival.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>22178201</pmid><doi>10.1016/j.neuropharm.2011.11.016</doi><tpages>8</tpages></addata></record> |
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subjects | Animals Behavior Callithrix Corpus Striatum - drug effects Corpus Striatum - metabolism Dopamine Dopamine - metabolism Dopaminergic Neurons - drug effects Dopaminergic Neurons - metabolism Female Male Marmoset MPTP MPTP Poisoning - drug therapy Neuroprotective Agents - pharmacology Neuroprotective Agents - therapeutic use Parkinson's disease Riluzole Riluzole - pharmacology Riluzole - therapeutic use Sleep Substantia Nigra - drug effects Substantia Nigra - metabolism |
title | Neuroprotective effects of riluzole in early phase Parkinson's disease on clinically relevant parameters in the marmoset MPTP model |
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